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Journal of Thrombosis and Haemostasis : JTH|October 10, 2024
Incidence and risk factors for postthrombotic syndrome in neonates and children in a single-center cohort studyIrene Klaassen, Sahinde Sari, Heleen van Ommen, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|September 21, 2021
Prophylaxis in children with haemophilia in an evolving treatment landscapeMaria Elisa Mancuso, Christoph Male, Gili Kenet, et al.Journal of Medical Internet Research|December 22, 2022
Patient-Centered Digital Health Records and Their Effects on Health Outcomes: Systematic ReviewMartijn R Brands, Samantha C Gouw, Molly Beestrum, et al.Thrombosis and Haemostasis|May 12, 2026
Thrombin Generation as a Potential Surrogate Marker of Hemostatic Status in the Era of Novel Therapies for HemophiliaYesim Dargaud, Giancarlo Castaman, Roberta Gualtierotti, et al.American Journal of Hematology|September 1, 2010
Development and validation of a pediatric severity index for sickle cell patientsXandra W van den Tweel, Johanna H van der Lee, Harriët Heijboer, et al.Thrombosis Research|November 5, 2013
Markers of endothelial dysfunction differ between subphenotypes in children with sickle cell diseaseVeronica van der Land, Marjolein Peters, Bart J Biemond, et al.Nederlands Tijdschrift Voor Geneeskunde|October 30, 2014
[Haemophilia]Janneke I Loomans, Janske Lock, Marjolein Peters, et al.Blood Reviews|July 19, 2017
To serve and protect: The modulatory role of von Willebrand factor on factor VIII immunogenicityRobin B Hartholt, Alice S van Velzen, Ivan Peyron, et al.Journal of Thrombosis and Haemostasis : JTH|April 12, 2026
Diagnosis and management of hemophilia A and BMing Y Lim, Jesús Ardila, Giancarlo Castaman, et al.Pediatric Blood & Cancer|September 5, 2009
Behavioral and emotional problems in children with sickle cell disease and healthy siblings: Multiple informants, multiple measuresChanna T Hijmans, Martha A Grootenhuis, Jaap Oosterlaan, et al.Pageof 16